Canonical Allele Identifier: CA432953555
Gene: GLB1 HGNC NCBI

Linked Data

gnomAD v4: 3-33021587-C-T
MyVariant Identifiers: chr3:g.33063079C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33021587C>T , CM000665.2:g.33021587C>T GRCh38
NC_000003.11:g.33063079C>T , CM000665.1:g.33063079C>T GRCh37
NC_000003.10:g.33038083C>T NCBI36
NG_009005.1:g.80616G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000307363.10:c.1212G>A MANE Select ENSP00000306920.4:p.Leu404=
ENST00000307363.9:c.1212G>A ENSP00000306920.4:p.Leu404=
ENST00000307377.12:c.819G>A ENSP00000305920.8:p.Leu273=
ENST00000399402.7:c.1122G>A ENSP00000382333.2:p.Leu374=
ENST00000461475.5:n.311G>A
ENST00000467571.5:n.249G>A
ENST00000473477.1:n.244G>A
ENST00000497796.5:n.464G>A
NM_000404.2:c.1212G>A NP_000395.2:p.Leu404=
NM_000404.3:c.1212G>A NP_000395.2:p.Leu404=
NM_001079811.1:c.1122G>A NP_001073279.1:p.Leu374=
NM_001079811.2:c.1122G>A NP_001073279.1:p.Leu374=
NM_001135602.1:c.819G>A NP_001129074.1:p.Leu273=
NM_001135602.2:c.819G>A NP_001129074.1:p.Leu273=
NM_001317040.1:c.1356G>A NP_001303969.1:p.Leu452=
XR_001740634.1:n.1543-601C>T
NM_000404.4:c.1212G>A MANE Select NP_000395.3:p.Leu404=
NM_001079811.3:c.1122G>A NP_001073279.2:p.Leu374=
NM_001135602.3:c.819G>A NP_001129074.2:p.Leu273=
NM_001317040.2:c.1356G>A NP_001303969.2:p.Leu452=
NM_001393580.1:c.1212G>A NP_001380509.1:p.Leu404=